MIM Software Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for additional automatically segmented contours and local deployment for Contour ProtégéAI, its robust AI auto-contouring solution

November 3, 2021 — MIM Software Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for additional automatically segmented contours and local deployment for Contour ProtégéAI, its robust AI auto-contouring solution.

MIM Software has received FDA 510(k) clearance for additional head and neck, thorax, prostate, and abdomen contours. Quality improvements to existing contours have also been implemented. 

Furthermore, Contour ProtégéAI now supports both cloud-hosted and local deployment in the United States.

"Contouring continues to be one of the most time-consuming tasks for radiation therapy clinics," said Andrew Nelson, Chief Executive Officer of MIM Software Inc. "MIM Software is dedicated to the continued development of Contour ProtégéAI to reduce the time required to contour and help clinics achieve quicker simulation to treatment times. This FDA 510(k) clearance significantly expands our offering and supports our ultimate goal of enhancing patient care."

Further enhancements will be pursued by MIM Software through additional FDA 510(k) clearances with the goal of pushing the capabilities of AI auto-contouring forward.

For more information: www.mimsoftware.com


Related Content

News | Stroke

March 11, 2026 — Brainomix, a provider of AI-powered imaging tools for stroke and lung fibrosis, has announced the ...

Time March 11, 2026
arrow
News | HIMSS

March 9, 2026 — Fujifilm Healthcare Americas Corp. is showcasing how its latest AI-powered enterprise imaging solutions ...

Time March 10, 2026
arrow
News | HIMSS

March 5, 2026 — At the Health Information and Management Systems Society (HIMSS) Conference & Exhibition 2026 in Las ...

Time March 06, 2026
arrow
News | Radiation Oncology

March 4, 2026 — Lunit has announced that 21 studies featuring its AI solutions will be presented at the European ...

Time March 05, 2026
arrow
News | Ultrasound Women's Health

March 2, 2026 — Ultrasound AI, a provider of artificial intelligence applications for medical imaging, has received FDA ...

Time March 03, 2026
arrow
News | FDA

Feb. 26, 2026 — The U.S. Food and Drug Administration (FDA) has given 510(k) class II clearance of qXR-Detect, the ...

Time February 26, 2026
arrow
News | Ultrasound Imaging

Feb. 25, 2026 — GE HealthCare is introducing the next generation of LOGIQ general imaging ultrasound systems – an ...

Time February 25, 2026
arrow
News | Women's Health

Feb.23, 2026 — The first clinical patient received a Clairity Breast cancer risk score, marking a historic milestone in ...

Time February 23, 2026
arrow
News | Magnetic Resonance Imaging (MRI)

Feb. 19, 2026 — GE HealthCare recently announced 510(k) clearance of three new magnetic resonance (MR) innovations with ...

Time February 20, 2026
arrow
News | Radiology Imaging

Feb. 12, 2026 — Siemens Healthineers and Mayo Clinic are expanding their strategic collaboration to enhance patient care ...

Time February 13, 2026
arrow
Subscribe Now